Improve access to specialist care

Trial ID
NCT05014971
Official Title
Multi-Stakeholder Engagement for Interdisciplinary Telehealth in Lewy Body Dementia
Goal
Improve access to specialist care
Phase
NA
Status
RECRUITING
Sponsor
University of Florida
Study Type
INTERVENTIONAL
Enrollment
106 participants
Conditions
Lewy Body Dementia With Behavioral Disturbance, Lewy Body Parkinson Disease, Lewy Body Disease
Interventions
Tele-neurohub

Summary For Families

The goal is to reduce behavioral disturbances and make coordinated, specialist care easier to access for people with Lewy body dementia. A "tele-neurohub" links an interdisciplinary team with the patient and an in-home caregiver over Zoom to assess symptoms, review and recommend medication adjustments such as weighing levodopa's motor benefits against possible hallucination risk, coach caregivers in behavior-management techniques, and plan follow-up care. The study seeks adults 18 to 100 with a clinician-confirmed diagnosis of mild to moderate Lewy body dementia, who have internet and a Zoom-compatible device, a caregiver living with them who will participate, and fluency in English.

Locations

  • University of Florida, Gainesville, Florida, United States

Frequently Asked Questions

What is this trial testing?
This trial is studying Tele-neurohub. The goal is to reduce behavioral disturbances and make coordinated, specialist care easier to access for people with Lewy body dementia. A "tele-neurohub" links an interdisciplinary team with the patient and an in-home caregiver over Zoom to assess symptoms, review and recommend medication adjustments such as weighing levodopa's motor benefits against possible hallucination risk, coach caregivers in behavior-management techniques, and plan follow-up care. The study seeks adults 18 to 100 with a clinician-confirmed diagnosis of mild to moderate Lewy body dementia, who have internet and a Zoom-compatible device, a caregiver living with them who will participate, and fluency in English.
Who can participate?
Participants must be between 18 Years and 100 Years.
Where is this trial located?
This trial is recruiting at 1 location.
Does it cost anything to join?
No. There is no cost to participate. Study-related care and treatment are provided at no charge.
How long does the trial last?
This trial is estimated to last approximately 4 years and 3 months.
Will I get the real drug or a placebo?
It depends on the trial design. Some Parkinson's trials are placebo controlled, meaning a portion of participants get an inactive comparison while others get the experimental treatment. Some use crossover designs so everyone eventually receives the active treatment at some point. Observational trials do not use a placebo at all because they are not testing a new treatment. The consent form for any specific trial spells out the design and your odds of being assigned to placebo before you enroll.
How often will I need to visit the study site?
Visit frequency varies by trial. Many Parkinson's studies require an in person visit every 4 to 12 weeks during the active treatment phase, with shorter or longer gaps depending on the design. The site coordinator can give you the full visit schedule before you sign anything, so you know what the time commitment looks like.
Can I leave the trial if I change my mind?
Yes. You can withdraw from any clinical trial at any time, for any reason, without affecting your standard medical care. Trials are voluntary by law. The team may ask if you are willing to do a brief exit visit so they can collect safety information, but you are not obligated.
Will travel or parking be reimbursed?
Many trials reimburse for parking, mileage, and sometimes lodging if the site is far from your home. Reimbursement policies vary by sponsor and site. When you contact the trial team, ask specifically what is covered and how reimbursement is processed.
Can my spouse or care partner come with me to visits?
In most cases yes, and it is often encouraged. Care partners can help with notes, questions, and getting home safely after a long visit. Some study assessments do need to happen one on one, but care partners are usually welcome for the rest of the appointment.

Related Reading

View on ClinicalTrials.gov